Publication: Storage of blood clots for histological analysis: how long is too long in saline and paraformaldehyde?
Authors
Douglas, Andrew ; Fitzgerald, Seán ; Pandit, Abhay ; Doyle, Karen M.
item.page.secondaryauthor
item.page.director
Publisher
Universidad de Murcia, Departamento de Biologia Celular e Histiologia
publication.page.editor
publication.page.department
DOI
https://doi.org/10.14670/HH-18-154
item.page.type
info:eu-repo/semantics/article
Description
Abstract
To investigate the composition of blood clots
following mechanical thrombectomy, it is essential to
ensure optimum storage for highest quality histological
and immunofluorescence analysis. We investigated for
how long clots can be stored in paraformaldehyde (PFA),
saline and heparinised saline before the tissue integrity is
compromised.
Whole blood and fibrin-rich clot analogues were
made under dynamic flow conditions. Clots were stored
in 4% PFA, saline or heparinised saline for timepoints
ranging from 1 hour to two months. Five μm sections
were stained with Martius Scarlet Blue to visualise red
blood cells (RBCs), white blood cells (WBCs) and
fibrin. Semi-quantitative analysis of the integrity of clot
components used a scoring system (0: Poor; 1: Sub-par;
2: High). Quantitative analysis used Orbit Image
Analysis software. Autofluorescence was assessed using
a relative scale.
Clots stored in PFA for up to two months were
qualitatively similar to those stored for all shorter
periods (median score: 2 per component). Clots stored in
saline/heparinised saline for one week showed
degradation of RBCs and WBCs, but fibrin remained
intact (median score: 1, 1, 2 respectively). Degradation
of the samples stored in saline/heparinised saline made
accurate quantification using Image Analysis software
difficult from 24h.
Samples stored in PFA for up to two weeks showed
an edging autofluorescence effect, which became more
evident with prolonged storage.
For optimum histology, ideally clots should not be
stored in saline before fixation and should ideally be
stored in formalin for less than one month to minimise
the impact of autofluorescence on immunofluorescence
publication.page.subject
Citation
Histology and Histopathology Vol. 35, nº 3 (2020)
item.page.embargo
Ir a Estadísticas
Este ítem está sujeto a una licencia Creative Commons. http://creativecommons.org/licenses/by-nc-nd/4.0/